Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01495507
Other study ID # Kuj-Germ-1
Secondary ID
Status Recruiting
Phase N/A
First received December 19, 2011
Last updated July 16, 2016
Start date November 2011

Study information

Verified date July 2016
Source Medical University Innsbruck
Contact Michael C Liebensteiner, MD, PhD
Phone +43 512 504 80547
Email michael.liebensteiner@i-med.ac.at
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Observational

Clinical Trial Summary

The field of patellofemoral disorders and accordant therapeutical interventions is a high turnover research field. It is important to verify the clinical outcome with appropriate measuring tools. There is evidence that the Kujala score is a reliable and widely used measuring instrument of patellofemoral disorders. Indeed, the Kujala score was already used in many studies investigating patellofemoral disorders - also in german speaking patient groups. Unfortunately, we are not aware of a validated german version of the Kujala score. Other relevant knee outcome scores were already successfully translated into german language and validated by previous investigators.

So, it is the aim of our study to cross-culturally adapt and then to validate the Kujala score for use in German-speaking individuals with patellofemoral instability. It is hypothesized that the german version of the Kujala score shows:

- High divergent construct validity as determined by significant differences between patients and controls (hypothesis 1)

- High convergent construct validity as determined by significant correlations with other relevant scoring systems (hypothesis 2)

- High reliability (hypothesis 3)

- High responsiveness (hypothesis 4)


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 70 Years
Eligibility Inclusion Criteria:

- german speaking

- MPFL-reconstruction planed

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Validation of Kujala Score German Version in Patients With Patellofemoral Instability and Scheduled MPFL-reconstruction

Intervention

Procedure:
MPFL- Reconstruction


Locations

Country Name City State
Austria Dept. Orthop. Surgery, Medical Univ. Innsbruck Innsbruck Tyrol

Sponsors (1)

Lead Sponsor Collaborator
Medical University Innsbruck

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Kujala Score 1 year No
Primary KOOS (Knee Injury and Osteoarthritis Outcome Score) 1 year No
Primary Marx Activity Scale 1 year No
Primary SF-12 (Short - Form 12) 1 year No
Primary VAS pain 1 year No
Primary Lysholm Score 1 year No